NDC 72059-001 Sting Relief Medicated Pad

Product Information

What is NDC 72059-001?

The NDC code 72059-001 is assigned by the FDA to the product Sting Relief Medicated Pad which is product labeled by Nantong Sirius Packing Products Co., Ltd.. The product's dosage form is and is administered via form. The product is distributed in a single package with assigned NDC code 72059-001-01 1 swab in 1 packet . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code72059-001
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Sting Relief Medicated Pad
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Nantong Sirius Packing Products Co., Ltd.
Labeler Code72059
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
02-01-2018
Listing Expiration Date What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
12-31-2019
Exclude Flag What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
I
NDC Code Structure

What are the uses for Sting Relief Medicated Pad?


Product Packages

NDC Code 72059-001-01

Package Description: 1 SWAB in 1 PACKET

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Sting Relief Medicated Pad Active Ingredients UNII Codes

NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

Sting Relief Medicated Pad Inactive Ingredients UNII Codes

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

* Please review the disclaimer below.

Sting Relief Medicated Pad Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Active Ingredient



Medicinal Ingredient:Benzocaine6%


Purpose



Topical Anesthetic


Use



For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites


Directions



Apply to affected area not more than 3 to 4 times daily. For adults and children 2 years of age and older. Children under 2 years: consult a physician. 


Warnings



FOR EXTERNAL USE ONLY.FLAMMABLE,Keep away from fire or flame.

Do not use in the eyes ,if contact occurs ,flush eyes with water.

other information sotre at room temperature 15 OC-30 OC(59-86 OF)


Otc - Keep Out Of Reach Of Children



KEEP OUT OF REACH OF CHILDREN. if swallowed get medical help or contact a Poison Control Center right away.


Inactive Ingredients



isopropyl alcohol,purified water


* Please review the disclaimer below.